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HIF: Basics Thomas Pogge and Miltos Ladikas University of Central Lancashire

HIF: Basics Thomas Pogge and Miltos Ladikas University of Central Lancashire. 0. Innova-P2 Objectives. Advance knowledge and ethical insight into reform plans for the current IPR system. Finalise the existing plan to amend the current IPR system in the area of pharmaceutical innovation.

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HIF: Basics Thomas Pogge and Miltos Ladikas University of Central Lancashire

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  1. HIF: Basics Thomas Pogge and MiltosLadikas University of Central Lancashire 0

  2. Innova-P2 Objectives • Advance knowledge and ethical insight into reform plans for the current IPR system. • Finalise the existing plan to amend the current IPR system in the area of pharmaceutical innovation. • Provide a reality check and obtain support for the new system from the world’s two most powerful emerging country actors (India and China). • Promote urgent policy developments on IPR by forging a consensus for the new system and providing a policy action plan.

  3. A Collaborative Project … Basic idea developed in 2003 independently by Aidan Hollis and Thomas Pogge, first peer-reviewed essay January 2005, then co-authored book in August 2008.

  4. Advisory Board of the HIF Project John J. DeGioia, President of Georgetown University Paul Farmer, co-founder of Partners in Health Jim Yong Kim, President of Dartmouth College Paul Martin, former Canadian Prime Minister Chris Murray, Director of Inst of Health Metrics James Orbinski, former Int’l President of MSF Baroness Onora O'Neill, British House of Lords Sir Michael Rawlins, Chair of NICE (UK) Karin Roth, MdB representing Esslingen AmartyaSen, Nobel Prize Winner in Economics HeidemarieWieczorek-Zeul, former German Minister 3

  5. Rules Governing the Development and Distribution of New Medicines Under the TRIPS agreement – part of the WTO Treaty – the intellectual property regime of the affluent countries was globalized by being made a mandatory condition of WTO membership. Pharmaceutical innovators must now be granted product patents of minimally 20-year duration in all WTO member states.

  6. Nine Problems with TRIPS-Pure 1.High prices impede accessby poor people for the duration of the patent Why are prices so high? Patented medicines for global diseases are priced to maximize profit (= mark-up times sales volume). For important medicines, optimal mark-up is high because of high economic inequality and low price elasticity among the affluent. 5

  7. Global Pharmaceutical Demand Curve

  8. Nine Problems with TRIPS-Pure 1. High prices impede access by the poor. 2. Pharmaceutical innovationis neglecting diseases concentrated among the poor. Why? Medicines for such diseases get stuck with either tiny mark-up or tiny sales volume.

  9. Distribution of Pharma Research Diseases accounting for 90% of the global disease burden receive only 10% of all medical research worldwide. The 10/90 Gap. Pneumonia, diarrhea, tuberculosis and malaria, which account for over 20% of the global burden of disease, receive less than 1%of all public and private funds devoted to health research. Of the 1556 new drugs approved between 1975 and 2004, only 18 were for tropical diseases and 3 for TB. www.plosone.org/article/info:doi/10.1371/journal.pone.0010610

  10. Nine Problems with TRIPS-Pure 1. High prices impeding access by the poor 2. Neglected diseases (90/10 Problem) 3. Excessive incentives toward me-too drugs 4. Too low rewards for real break-throughs 5. Bias toward maintenance drugs 6. Patenting, litigation, deadweight losses 7. Cost-price diff’l excessive marketing 8. Cost-price differential  counterfeiting 9. Last-mile problem, perverse incentives

  11. The Health Impact Fund (HIF) … is a complementto TRIPS. Innovators may voluntarilyregister any new medicine with the HIF. … promises to reward (upon registration) any new medicine annually for ten years on the basis of its global health impact(in QALYs). … is funded by willing governments at initially $6 billion per annum (0.01% of ΣGNI). Registrant gives up no intellectual property rights but agrees to sell the new medicine wherever it is needed at the lowest feasible average cost of manufacture and distribution and to grant zero-priced licenses after reward period. 11

  12. The HIF Avoids Three Critical Problems in Prize Determination Which health problems to target; how to define the “finish line”; how large to make the reward (self-adjusting). The HIF is a market-based solution: payments are determined by competition among all registered products for the available reward pools. A drug for malaria can directly compete against a drug  for HIV/AIDS. This regulates relative rewards for registered products, rewarding each at the same rate per unit of health impact and thereby creating efficient incentives. 12

  13. The HIF Tackles all 9 Problems 1. All HIF-registered products are available at or below cost from Day One. The poor get better access to important new medicines: through their own funds or through national governments, international agencies, or NGOs. 2. The HIF provides powerful new incentives to develop new medicines with the greatest health impact — regardless of whether the patient population that will benefit is rich or poor. 13

  14. 9. The HIF Alleviates Last Mile Problems in Drug Delivery Local availability as well as proper storage, prescribing and compliance are essential to drug effectiveness. Dilemma: drugs are either too expensive or “too cheap,” hence unaffordable or unpromoted, among the poor. The HIF pays on the basis of each medicine’s actual health impact as assessed through sampling of actual use & benefits as well as through population health data. Firms therefore have incentives to promote appropriate use of their registered products, as well as to develop products that are effective in resource-poor settings. 14

  15. Financing $6 billion a year is about 0.01% of global income (ΣGNI), well under 1% of current worldwide expenditures on pharmaceuticals. Full incentive effects on potential innovators require long-term commitment by funders. Only governments (of affluent and middle income countries) can plausibly commit large sums long-term. We propose a small share of GNI, perhaps 0.03%, for each partner country. All or most of this comes back to taxpayers through lower prices for medicines, insurance, national health systems, and foreign aid. 15

  16. Next Steps Piloting the HIF Finalise impact assessment issues Work with similarly minded initiatives (e.g. Global Fund) Work with willing governments (e.g. Germany, India, China) 16

  17. Thank you! www.HealthImpactFund.org 17

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